| Literature DB >> 30169568 |
Yan Zhao1, Yujie Ning1,2, Feng Zhang1, Miao Ding1, Yan Wen1, Liang Shi2, Kunpeng Wang2, Mengnan Lu2, Jingyan Sun2, Menglu Wu2, Bolun Cheng1, Mei Ma1, Lu Zhang1, Shiqiang Cheng1, Hui Shen3, Qing Tian3, Xiong Guo1, Hong-Wen Deng3.
Abstract
Genetic risk score (GRS, also known as polygenic risk score) analysis is an increasingly popular method for exploring genetic architectures and relationships of complex diseases. However, complex diseases are usually measured by multiple correlated phenotypes. Analyzing each disease phenotype individually is likely to reduce statistical power due to multiple testing correction. In order to conquer the disadvantage, we proposed a principal component analysis (PCA)-based GRS analysis approach. Extensive simulation studies were conducted to compare the performance of PCA-based GRS analysis and traditional GRS analysis approach. Simulation results observed significantly improved performance of PCA-based GRS analysis compared to traditional GRS analysis under various scenarios. For the sake of verification, we also applied both PCA-based GRS analysis and traditional GRS analysis to a real Caucasian genome-wide association study (GWAS) data of bone geometry. Real data analysis results further confirmed the improved performance of PCA-based GRS analysis. Given that GWAS have flourished in the past decades, our approach may help researchers to explore the genetic architectures and relationships of complex diseases or traits.Entities:
Keywords: bioinformatics; complex diseases; correlation analysis; genetic risk score; principal component analysis
Mesh:
Year: 2019 PMID: 30169568 PMCID: PMC6954421 DOI: 10.1093/bib/bby075
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622